Variant report

Variant	nsv870821
Chromosome Location	chr1:103339272-103379918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:103344992-103345640	HCT-116	colon:	n/a	n/a
2	CEBPB	chr1:103344973-103345668	HCT-116	colon:	n/a	n/a
3	CEBPB	chr1:103344985-103345539	A549	lung:	n/a	n/a
4	CEBPB	chr1:103344992-103345511	A549	lung:	n/a	n/a
5	CEBPB	chr1:103344931-103345570	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:103344959-103345583	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:103363004-103363495	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:103363066-103363488	A549	lung:	n/a	n/a
9	CHD2	chr1:103363173-103363438	Hela-S3	cervix:	n/a	n/a
10	E2F4	chr1:103345178-103345411	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr1:103379321-103379492	MCF10A-Er-Src	breast:	n/a	n/a
12	EBF1	chr1:103354364-103354554	GM12878	blood:	n/a	chr1:103354472-103354483
13	EP300	chr1:103344887-103345739	SK-N-SH	brain:	n/a	chr1:103344934-103344948 chr1:103344928-103344942
14	EP300	chr1:103357391-103358384	SK-N-SH	brain:	n/a	n/a
15	EP300	chr1:103363020-103363602	SK-N-SH	brain:	n/a	n/a
16	EP300	chr1:103363076-103363463	Hela-S3	cervix:	n/a	n/a
17	EP300	chr1:103363099-103363337	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr1:103357417-103358172	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr1:103357430-103358192	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr1:103344999-103345583	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr1:103345125-103345545	Hela-S3	cervix:	n/a	n/a
22	EP300	chr1:103361815-103362435	SK-N-SH	brain:	n/a	n/a
23	EP300	chr1:103344989-103345539	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr1:103363065-103363695	SK-N-SH	brain:	n/a	n/a
25	ESR1	chr1:103341323-103341587	ECC-1	luminal epithelium:	n/a	n/a
26	ESR1	chr1:103341335-103341622	ECC-1	luminal epithelium:	n/a	n/a
27	FOS	chr1:103357578-103358133	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
28	FOS	chr1:103363119-103363644	HUVEC	blood vessel:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
29	FOS	chr1:103347402-103347740	HUVEC	blood vessel:	n/a	chr1:103347522-103347533 chr1:103347527-103347534 chr1:103347531-103347540 chr1:103347526-103347534
30	FOS	chr1:103363109-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
31	FOS	chr1:103363093-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
32	FOS	chr1:103345171-103345538	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:103363102-103363463	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
34	FOS	chr1:103357453-103358283	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
35	FOS	chr1:103363063-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
36	FOS	chr1:103345058-103345531	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:103363053-103363472	Hela-S3	cervix:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
38	FOS	chr1:103345100-103345650	HUVEC	blood vessel:	n/a	n/a
39	FOS	chr1:103345162-103345513	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:103357663-103358117	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
41	FOS	chr1:103357659-103358082	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
42	FOS	chr1:103357677-103358543	HUVEC	blood vessel:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
43	FOS	chr1:103345030-103345551	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL1	chr1:103357702-103358130	HCT-116	colon:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
45	FOSL1	chr1:103345143-103345515	HCT-116	colon:	n/a	n/a
46	FOSL1	chr1:103344949-103345615	HCT-116	colon:	n/a	n/a
47	FOSL2	chr1:103363068-103363361	A549	lung:	n/a	chr1:103363274-103363281
48	FOSL2	chr1:103363083-103363499	MCF-7	breast:	n/a	chr1:103363274-103363281
49	FOSL2	chr1:103357546-103358078	A549	lung:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
50	FOSL2	chr1:103363041-103363377	MCF-7	breast:	n/a	chr1:103363274-103363281

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103343469-103343519	NHDF-neo	bronchial:	n/a
2	chr1:103343469-103343519	SK-N-SH	brain:	n/a
3	chr1:103343469-103343519	AG10803	skin:	n/a
4	chr1:103343469-103343519	NHBE	bronchial:	n/a
5	chr1:103343469-103343519	HCM	heart:	n/a
6	chr1:103343469-103343519	GM06990	blood:	n/a
7	chr1:103343469-103343519	NH-A	brain:	n/a
8	chr1:103343469-103343519	HIPEpiC	eye:	n/a
9	chr1:103343469-103343519	GM12892	blood:	n/a
10	chr1:103343469-103343519	AG09309	skin:	n/a
11	chr1:103343469-103343519	BE2_C	brain:	n/a
12	chr1:103343469-103343519	ProgFib	skin:	n/a
13	chr1:103343469-103343519	CMK	blood:	n/a
14	chr1:103343469-103343519	BJ	skin:	n/a
15	chr1:103343469-103343519	Caco-2	colon:	n/a
16	chr1:103343469-103343519	AoSMC	blood vessel:	n/a
17	chr1:103343469-103343519	SAEC	small airway:	n/a
18	chr1:103343469-103343519	HMEC	breast:	n/a
19	chr1:103343469-103343519	Hepatocyte	liver:	n/a
20	chr1:103343469-103343519	SK-N-MC	brain:	n/a
21	chr1:103343469-103343519	HCPEpiC	choroid plexus:	n/a
22	chr1:103343469-103343519	HL-60	blood:	n/a
23	chr1:103343469-103343519	HCF	heart:	n/a
24	chr1:103343469-103343519	HEK293	kidney:	embryo
25	chr1:103343469-103343519	SKMC	muscle:	n/a
26	chr1:103343469-103343519	AG09319	gingival:	n/a
27	chr1:103343469-103343519	ECC-1	luminal epithelium:	n/a
28	chr1:103343469-103343519	HRCEpiC	kidney:	n/a
29	chr1:103343469-103343519	HepG2	liver:	n/a
30	chr1:103343469-103343519	HRPEpiC	eye:	n/a
31	chr1:103343469-103343519	Jurkat	blood:	n/a
32	chr1:103343469-103343519	GM19239	blood:	n/a
33	chr1:103343469-103343519	HEEpiC	esophagus:	n/a
34	chr1:103343469-103343519	T-47D	breast:	n/a
35	chr1:103343469-103343519	U87	brain:	n/a
36	chr1:103343469-103343519	NB4	blood:	n/a
37	chr1:103343469-103343519	PrEC	prostate:	n/a
38	chr1:103343469-103343519	MCF10A-Er-Src	breast:	n/a
39	chr1:103343469-103343519	AG04450	lung:	fetal
40	chr1:103343469-103343519	NT2-D1	testis:	n/a
41	chr1:103343469-103343519	GM12878	blood:	n/a
42	chr1:103343469-103343519	ovcar-3	ovarian:	n/a
43	chr1:103343469-103343519	RPTEC	kidney:	n/a
44	chr1:103343469-103343519	K562	blood:	n/a
45	chr1:103343469-103343519	H1-hESC	embryonic stem cell:	embryo
46	chr1:103343469-103343519	MCF-7	breast:	n/a
47	chr1:103343469-103343519	AG04449	skin:	fetal
48	chr1:103343469-103343519	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:103343469-103343519	PFSK-1	brain:	n/a
50	chr1:103343469-103343519	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:
2	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:

Variant related genes	Relation type
COL11A1	TF binding region
COL11A1	CpG island

Extended variants
information (count: 1638 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55785630	chr1:103339272-103339273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34837345	chr1:103339284-103339285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61108225	chr1:103339298-103339299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377417071	chr1:103339356-103339357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182751022	chr1:103339357-103339358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537101332	chr1:103339360-103339361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11420293	chr1:103339369-103339370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555837635	chr1:103339372-103339373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368436964	chr1:103339378-103339379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370772146	chr1:103339398-103339399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78467903	chr1:103339468-103339469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559992292	chr1:103339528-103339529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6680329	chr1:103339576-103339577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542585653	chr1:103339586-103339587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114649404	chr1:103339589-103339590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563709588	chr1:103339695-103339696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531342621	chr1:103339709-103339710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375910036	chr1:103339739-103339740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188118838	chr1:103339742-103339743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370111592	chr1:103339789-103339790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561862029	chr1:103339821-103339822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529462747	chr1:103339855-103339856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116079477	chr1:103339896-103339897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191386494	chr1:103339902-103339903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540105975	chr1:103339908-103339909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552125971	chr1:103339923-103339924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569908563	chr1:103339959-103339960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537492072	chr1:103339974-103339975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555574398	chr1:103339992-103339993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548433472	chr1:103340076-103340077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535256364	chr1:103340129-103340130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183639484	chr1:103340188-103340189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553415992	chr1:103340209-103340210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78503474	chr1:103340210-103340211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545647744	chr1:103340216-103340217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545544167	chr1:103340217-103340218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558043014	chr1:103340223-103340224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187532983	chr1:103340231-103340232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192002287	chr1:103340232-103340233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543451667	chr1:103340243-103340244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61813898	chr1:103340253-103340254	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs113030571	chr1:103340257-103340258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541145365	chr1:103340266-103340267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575788017	chr1:103340267-103340268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562220862	chr1:103340320-103340321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564617700	chr1:103340405-103340406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533573125	chr1:103340406-103340407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543215394	chr1:103340407-103340408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375847767	chr1:103340436-103340437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114893499	chr1:103340440-103340441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103334000-103349800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:103335400-103350000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:103338200-103340000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:103338400-103342800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr1:103338400-103343400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:103338400-103369400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:103338600-103342600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:103338600-103345000	Weak transcription	NH-A	brain
9	chr1:103338800-103357200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:103339000-103342600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:103339000-103345000	Weak transcription	HSMM	muscle
12	chr1:103339200-103349800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:103340000-103345200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:103340800-103350000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:103341400-103345000	Weak transcription	HSMMtube	muscle
16	chr1:103341400-103349800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:103341600-103352000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:103342400-103349800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:103342600-103345200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:103342600-103345200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:103342800-103346000	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:103343000-103345800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:103343400-103345000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:103343400-103352000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:103343400-103355800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:103343400-103356200	Weak transcription	Fetal Heart	heart
27	chr1:103343400-103366000	Weak transcription	Fetal Brain Female	brain
28	chr1:103344400-103349800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:103344600-103345000	Enhancers	A549	lung
30	chr1:103344800-103345000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:103344800-103345000	Enhancers	Osteobl	bone
32	chr1:103344800-103345600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:103345000-103345200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:103345000-103345200	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:103345000-103345200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr1:103345000-103345400	Flanking Active TSS	NH-A	brain
37	chr1:103345000-103345600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:103345000-103345600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:103345000-103345600	Flanking Active TSS	A549	lung
40	chr1:103345000-103345600	Enhancers	Hela-S3	cervix
41	chr1:103345000-103345600	Enhancers	HSMMtube	muscle
42	chr1:103345000-103345600	Flanking Active TSS	Osteobl	bone
43	chr1:103345000-103345800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:103345000-103345800	Enhancers	NHDF-Ad	bronchial
45	chr1:103345000-103346000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:103345000-103346000	Enhancers	HSMM	muscle
47	chr1:103345000-103346000	Enhancers	NHLF	lung
48	chr1:103345000-103346400	Enhancers	HMEC	breast
49	chr1:103345000-103348000	Enhancers	HUVEC	blood vessel
50	chr1:103345200-103345400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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